Variant report

Variant rs17110887
Chromosome Location chr1:94493299-94493300
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94488000-94496600 Weak transcription Lung lung
2 chr1:94488200-94505000 Weak transcription Spleen Spleen
3 chr1:94488400-94493400 Weak transcription Placenta Placenta
4 chr1:94488600-94502600 Weak transcription Right Atrium heart
5 chr1:94489200-94493800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
6 chr1:94490800-94494200 Enhancers HMEC breast
7 chr1:94491200-94494200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:94491400-94494000 Enhancers NHEK skin
9 chr1:94491400-94499000 Enhancers HepG2 liver
10 chr1:94491600-94494400 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr1:94491600-94496600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr1:94491800-94496600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
13 chr1:94492000-94496400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr1:94492200-94496000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr1:94492200-94497200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr1:94492200-94510000 Weak transcription Aorta Aorta
17 chr1:94492800-94498600 Weak transcription GM12878-XiMat blood
18 chr1:94493000-94497200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
19 chr1:94493200-94493800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
20 chr1:94493200-94494000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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